- Merck & Co. (Rahway, NJ)
- …and Validation Specialist position available at the Rahway, New Jersey research facility . The Metrology and Validation Specialist will work as part of the ... Job DescriptionTitle: Specialist , Metrology and Validation, Analytical Research & DevelopmentJob Description-The Analytical Research & Development (AR&D) External… more
- Merck & Co. (Rahway, NJ)
- …Jersey and reports to the Sterile Process Engineering Lead of the FLEx GMP facility within Pharmaceutical Operations and Clinical Supply (PSCS).- Education ... independent problem-solving. Preferred Experience and Skills: Experience with sterile GMP facility startup.Knowledge of Investigational drug regulatory… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Small-Scale Organics (SSO) Pilot Plant is a GMP (Good Manufacturing Practices) manufacturing facility in the Small Molecule Process Research ... overall SM PR&D pipeline. Responsibilities: Under the scientific direction of a facility lead, the Operations Specialist will participate in equipment setups,… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …support of computer systems validation, equipment, utilities, and facility qualification, process validation, shipping validation, and data integrity.Key ... treatment of multiple myeloma.Legend Biotech is seeking QA Validation Specialist III as part of the Quality team based...and processes within a cell therapy manufacturing plant to support both clinical and commercial requirements in a sterile… more
- Aequor (Thousand Oaks, CA)
- …work alongside other innovative, driven professionals in this meaningful role. Role: Specialist Manufacturing, New Product Introduction Let's do this! At we strive ... critical role for the Thousand Oaks Drug Product (DP) facility , - also known as ATO B20 - you...introduction of new products into the manufacturing plant. This " Specialist Manufacturing" role will serve as a New Product… more
- Eisai, Inc (Raleigh, NC)
- …difference. If this is your profile, we want to hear from you. The QA Specialist plays a critical role in ensuring the quality and compliance of commercial and ... clinical products manufactured at the Eisai Raleigh facility . This position is responsible for executing core quality assurance functions, supporting regulatory… more
- Merck & Co. (Rahway, NJ)
- …Clinical Finished Goods).- - Responsible for authoring clinical supply documentation in support of labeling and packaging activities as well as supply chain ... documentation to support critical CMC activities . - Responsible for authoring.../ portfolio management. - Knowledge of Good Manufacturing Practices ( GMP ) and Good Clinical Practices (GCP) is highly desirable.… more
- Merck & Co. (Rahway, NJ)
- …forecast for CFGs is maintained. --Report clinical supply chain incidents to support the gathering of metrics in GCS to describe business health. Participate ... areas for operational improvement.-Participates in critical non-pipeline activities in support of clinical supply planning group (eg, process improvement… more
- Merck & Co. (Durham, NC)
- …the Durham sites.- This includes Energy Center, Vaccine Bulk and Manufacturing Facilities , Quality Labs, Material Management Storage Facility (MMSF) and projects ... Arrangements:Not ApplicableShift:1st - DayValid Driving License:NoHazardous Material(s):n/aRequired Skills:Equipment Qualification, Facility Management, Good Manufacturing Practices ( GMP ), Maintenance… more
- Merck & Co. (Durham, NC)
- …Vaccine Bulk and Manufacturing Facilities , Quality Labs, Material Management Storage Facility (MMSF) and projects. At times, support may extend to the ... manufacturer? If so, then this is the opportunity for you!The Associate Specialist , Calibration is a member of the Engineering, Maintenance and Site Services… more
- Merck & Co. (Durham, NC)
- …control, data collection techniques, and troubleshooting in compliance with SDLC, GMP , safety, and environmental regulations.- Actively support , participate and ... Job DescriptionThe Associate Specialist , is a member of the Site Automation...team responsible for the assigned process control systems in support of manufacturing operations located in Durham, NC.This Individual… more
- ThermoFisher Scientific (Cincinnati, OH)
- … III is responsible for collaborating with a team of QA personnel supporting GMP facilities and utilities used in drug product manufacturing, at Thermo Fisher ... Standard (Mon-Fri) **Environmental Conditions** Adherence to all Good Manufacturing Practices ( GMP ) Safety Standards, Office **Job Description** When you're part of… more
- Merck (Wilson, NC)
- …Energy Center, Vaccine Manufacturing Facility , Quality Labs, and a Packaging facility . This support position will focus on investigation of utility/ ... Management, Change Management, Data Analysis, Deviation Management, Equipment Qualification, Facility Management, GMP Compliance, Good Manufacturing Practices (… more
- PCI Pharma Services (Bedford, NH)
- …and Visual Inspection activities for clinical and commercial drug product in a GMP facility . The work scope includes on-the-floor Quality oversight of ... and shape the future of PCI. The QA Operations Specialist II - Floor Support is responsible...performing AQL visual inspection of finished drug product vials, GMP documentation and Batch Record review, line clear and… more
- Catalent Pharma Solutions (Harmans, MD)
- The **Senior Specialist , QA Client Support ** is responsible for providing QA support to Client Projects from start to finish for GMP Manufacturing of ... The general specialist is responsible for ensuring compliance to regulatory, GMP and industry standards. This role is responsible for review of quality… more
- Merck (Rahway, NJ)
- …Jersey and reports to the Sterile Process Engineering Lead of the FLEx GMP facility within Pharmaceutical Operations and Clinical Supply (PSCS). **Education ... independent problem-solving. **Preferred Experience and Skills:** + Experience with sterile GMP facility startup. + Knowledge of Investigational drug regulatory… more
- Merck (Rahway, NJ)
- …and Validation Specialist position available at the Rahway, New Jersey research facility . The Metrology and Validation Specialist will work as part of the ... **Job Description** **Title: Specialist ,** **Metrology and Validation, Analytical Research & Development**...routine maintenance of analytical equipment and instrumentation within the GMP environment. The key responsibilities of this role will… more
- Nestle (Jonesboro, AR)
- …position is not eligible for Visa Sponsorship._ **Position Overview:** As a Quality Specialist , you will perform a variety of quality control tests and inspections, ... company Quality Policy on all required Good Manufacturing Practices ( GMP ), quality and food safety requirements + Escalate quality...+ May be responsible for Net Contents Control system support & reporting + Supports the functionality of the… more
- Nestle (Burlington, WI)
- …eligible for Visa Sponsorship._ **POSITION SUMMARY** : The Factory Quality Specialist performs a variety of quality control tests/inspections and/or standard ... CPARs from Internal Audit Team and Third Party Audits- Support traceability exercises + Members of Internal Audit Team...follow and carry out company policy on all required GMP , quality and food safety requirements and escalate quality… more
- Merck (De Soto, KS)
- …Assurance Specialist role is responsible for providing guidance and support to implement, execute, and oversee compliance and quality-related processes in ... accordance with applicable GMP requirements and our company's Animal Health Quality Systems....quality management, and warehouse areas, and will provide overall support with quality audit (internal and external). **Other expectations… more
